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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA04g09140	A04	6486909	C	T	downstream_gene_variant	MODIFIER	c.*3046G>A\|	S39
2	BAA04g09140	A04	6487088	G	A	downstream_gene_variant	MODIFIER	c.*2867C>T\|	S36
3	BAA04g09140	A04	6487129	C	T	downstream_gene_variant	MODIFIER	c.*2826G>A\|	S174 S27
4	BAA04g09140	A04	6487139	C	T	downstream_gene_variant	MODIFIER	c.*2816G>A\|	S283
5	BAA04g09140	A04	6487156	C	T	downstream_gene_variant	MODIFIER	c.*2799G>A\|	S95
6	BAA04g09140	A04	6487231	C	T	downstream_gene_variant	MODIFIER	c.*2724G>A\|	S7
7	BAA04g09140	A04	6487305	C	T	downstream_gene_variant	MODIFIER	c.*2650G>A\|	S224
8	BAA04g09140	A04	6487324	C	T	downstream_gene_variant	MODIFIER	c.*2631G>A\|	S303
9	BAA04g09140	A04	6487367	G	A	downstream_gene_variant	MODIFIER	c.*2588C>T\|	S60
10	BAA04g09140	A04	6487390	G	A	downstream_gene_variant	MODIFIER	c.*2565C>T\|	S5
11	BAA04g09140	A04	6487429	C	T	downstream_gene_variant	MODIFIER	c.*2526G>A\|	S157 S163
12	BAA04g09140	A04	6488771	G	A	downstream_gene_variant	MODIFIER	c.*1184C>T\|	S161
13	BAA04g09140	A04	6488922	C	T	downstream_gene_variant	MODIFIER	c.*1033G>A\|	S9
14	BAA04g09140	A04	6489085	T	A	downstream_gene_variant	MODIFIER	c.*870A>T\|	S174 S27
15	BAA04g09140	A04	6489820	G	A	downstream_gene_variant	MODIFIER	c.*135C>T\|	S219 S72
16	BAA04g09140	A04	6489828	C	T	downstream_gene_variant	MODIFIER	c.*127G>A\|	S168
17	BAA04g09140	A04	6490105	C	A	synonymous_variant	LOW	c.510G>T\|p.Thr170Thr	S226 S238 S267
18	BAA04g09140	A04	6490117	A	T	synonymous_variant	LOW	c.498T>A\|p.Ala166Ala	S213 S226 S238 S257 S267
19	BAA04g09140	A04	6490120	A	G	synonymous_variant	LOW	c.495T>C\|p.Ile165Ile	S213 S226 S238 S257 S267
20	BAA04g09140	A04	6490126	A	T	synonymous_variant	LOW	c.489T>A\|p.Pro163Pro	S213 S226 S238 S257 S267
21	BAA04g09140	A04	6490144	C	A	synonymous_variant	LOW	c.471G>T\|p.Ser157Ser	S201 S213 S226 S238 S257 S267
22	BAA04g09140	A04	6490153	T	A	synonymous_variant	LOW	c.462A>T\|p.Gly154Gly	S201 S213 S226 S238 S257 S267
23	BAA04g09140	A04	6490162	A	G	synonymous_variant	LOW	c.453T>C\|p.Thr151Thr	S201 S213 S226 S238 S257 S267
24	BAA04g09140	A04	6490189	A	C	synonymous_variant	LOW	c.426T>G\|p.Leu142Leu	S14 S201 S213 S220 S238 S239 S257 S267
25	BAA04g09140	A04	6490198	G	C	synonymous_variant	LOW	c.417C>G\|p.Ala139Ala	S14 S201 S213 S220 S238 S239 S257 S267

Users can query the SNP information according to the gene ID.